Time-Resolved Coulomb Explosion Imaging Unveils Ultrafast Ring Opening of Furan

Enliang Wang, Surjendu Bhattacharyya, Keyu Chen, Kurtis Borne, Farzaneh Ziaee, Shashank Pathak, Huynh Van Sa Lam, Anbu Selvam Venkatachalam, Xiangjun Chen, Rebecca Boll, Till Jahnke, Artem Rudenko, Daniel Rolles
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Abstract

Following the changes in molecular structure throughout the entirety of a chemical reaction with atomic resolution is a long-term goal in femtochemistry. Although the development of a plethora of ultrafast technique has enabled detailed investigations of the electronic and nuclear dynamics on femtosecond time scales, direct and unambiguous imaging of the nuclear motion during a reaction is still a major challenge. Here, we apply time-resolved Coulomb explosion imaging with femtosecond near-infrared pulses to visualize the ultraviolet-induced ultrafast molecular dynamics of gas-phase furan. Widely contradicting predictions and observations for this molecule have been reported in the literature. By combining the experimental Coulomb explosion imaging data with ab initio molecular dynamics and Coulomb explosion simulations, we reveal the presence of a strong ultrafast ring-opening pathway upon excitation at 198 nm that occurs within 100 fs.
时间分辨库仑爆炸成像揭示了呋喃的超快开环
用原子分辨率跟踪整个化学反应过程中分子结构的变化是飞化学的一个长期目标。尽管大量超快技术的发展使得在飞秒时间尺度上对电子和核动力学进行详细的研究成为可能,但在反应过程中对核运动进行直接和明确的成像仍然是一个重大挑战。本文采用飞秒近红外脉冲时间分辨库仑爆炸成像技术,对紫外诱导气相呋喃的超快分子动力学进行了可视化研究。文献中对这种分子的预测和观察结果相互矛盾。通过将实验库仑爆炸成像数据与从头算分子动力学和库仑爆炸模拟相结合,我们揭示了在100fs内发生在198nm激发时的强超快开环路径的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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